about
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BPA new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stabilityTwo-stage translational control of dentate gyrus LTP consolidation is mediated by sustained BDNF-TrkB signaling to MNKDendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational controlLimitations in predicting PAM50 intrinsic subtype and risk of relapse score with Ki67 in estrogen receptor-positive HER2-negative breast cancer.FMRP and its target RNAs: fishing for the specificity.BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapsesThe fragile X protein binds mRNAs involved in cancer progression and modulates metastasis formation.Reelin expression in human liver of patients with chronic hepatitis C infection.Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations.Atrial natriuretic peptide effects on intracellular pH changes and ROS production in HEPG2 cells: role of p38 MAPK and phospholipase D.The nuclear RNA-binding protein Sam68 translocates to the cytoplasm and associates with the polysomes in mouse spermatocytes.Differential sensitivity of human monocytes and macrophages to ANP: a role of intracellular pH on reactive oxygen species production through the phospholipase involvement.Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.Another view of the role of FMRP in translational regulation.
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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label
F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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F Zalfa
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P108
P106
P108
P1153
57193699343
6602368386
P31
P496
0000-0002-1922-9468